Canonical Allele Identifier: PA310054
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu17927Pro
CA310052
NM_001267550.2:c.53780T>C